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Gene: ZNF629 (zinc finger protein 629) Homo sapiens

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Symbol:

ZNF629

Name:

zinc finger protein 629

RGD ID:

1314773

HGNC Page

HGNC:29008

Description:

Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

DNA-binding protein; KIAA0326; zinc finger protein 65; ZNF; ZNF65

RGD Orthologs

Alliance Orthologs

More Info

more info ...

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	16	30,778,456 - 30,787,205 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	16	30,778,456 - 30,787,205 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	16	30,789,777 - 30,798,526 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	16	30,697,271 - 30,706,024 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	16	29,498,892 - 29,507,651 (+)	NCBI		Celera
Cytogenetic Map	16	p11.2	NCBI
HuRef	16	28,352,601 - 28,361,366 (-)	NCBI		HuRef
CHM1_1	16	32,106,931 - 32,115,684 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	16	31,165,899 - 31,174,664 (-)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

branched-chain keto acid dehydrogenase kinase deficiency (IAGP)

dilated cardiomyopathy (IAGP)

generalized epilepsy with febrile seizures plus 9 (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

1,2-dimethylhydrazine (ISO)

2,3,7,8-tetrachlorodibenzodioxine (ISO)

3,4-methylenedioxymethamphetamine (ISO)

4,4'-sulfonyldiphenol (ISO)

acrylamide (EXP)

benzo[a]pyrene (ISO)

benzo[e]pyrene (EXP)

bisphenol A (ISO)

C60 fullerene (ISO)

carbon nanotube (ISO)

cobalt dichloride (ISO)

copper(II) sulfate (EXP)

crocidolite asbestos (ISO)

cyclosporin A (EXP)

dicrotophos (EXP)

enzyme inhibitor (EXP)

ethanol (ISO)

FR900359 (EXP)

gentamycin (ISO)

hydrogen cyanide (ISO)

iron dichloride (EXP)

lead(0) (EXP)

leflunomide (EXP)

methapyrilene (EXP)

perfluorohexanesulfonic acid (EXP)

perfluorononanoic acid (EXP)

perfluorooctane-1-sulfonic acid (EXP)

perfluorooctanoic acid (EXP)

pirinixic acid (ISO)

potassium cyanide (ISO)

sodium arsenite (EXP)

titanium dioxide (ISO)

troglitazone (ISO)

trovafloxacin (ISO)

urethane (EXP)

valproic acid (EXP)

zidovudine (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

regulation of transcription by RNA polymerase II (IBA)

Cellular Component

nucleus (IBA,IEA)

Molecular Function

DNA binding (IEA)

protein binding (IPI)

zinc ion binding (IEA)

References

References - curated

#	Reference Title	Reference Citation
1.	GOAs Human GO annotations	GOA_HUMAN data from the GO Consortium
2.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:1505991	PMID:1946370	PMID:9205841	PMID:12477932	PMID:18029348	PMID:21873635	PMID:23449627	PMID:25281560	PMID:25921289	PMID:26186194	PMID:26496610	PMID:28514442
PMID:28695742	PMID:29180619	PMID:29395067	PMID:29507755	PMID:29802200	PMID:29844126	PMID:30209976	PMID:30804502	PMID:31091453	PMID:31753913	PMID:32239614	PMID:32296183
PMID:32694731	PMID:32807901	PMID:32891193	PMID:33961781	PMID:34079125	PMID:34189442	PMID:34244482	PMID:35013218	PMID:35140242	PMID:35271311	PMID:35563538	PMID:35850772
PMID:35915203	PMID:35944360	PMID:36168627	PMID:36232890	PMID:36537216	PMID:36931259	PMID:37059091	PMID:37267103	PMID:38580884	PMID:38697112	PMID:38777146

Genomics

Comparative Map Data

ZNF629
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	16	30,778,456 - 30,787,205 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	16	30,778,456 - 30,787,205 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	16	30,789,777 - 30,798,526 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	16	30,697,271 - 30,706,024 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Celera	16	29,498,892 - 29,507,651 (+)	NCBI		Celera
Cytogenetic Map	16	p11.2	NCBI
HuRef	16	28,352,601 - 28,361,366 (-)	NCBI		HuRef
CHM1_1	16	32,106,931 - 32,115,684 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	16	31,165,899 - 31,174,664 (-)	NCBI		T2T-CHM13v2.0

Zfp629
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	7	127,206,203 - 127,215,053 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	7	127,206,203 - 127,214,969 (-)	Ensembl		GRCm39 Ensembl
GRCm38	7	127,607,028 - 127,615,785 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	7	127,607,031 - 127,615,797 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	7	134,750,549 - 134,757,947 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	7	127,398,183 - 127,405,581 (-)	NCBI		MGSCv36	mm8
Celera	7	127,451,941 - 127,459,339 (-)	NCBI		Celera
Cytogenetic Map	7	F3	NCBI
cM Map	7	69.62	NCBI

Zfp629
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	1	191,648,753 - 191,689,082 (-)	NCBI		GRCr8
mRatBN7.2	1	182,217,499 - 182,258,585 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	1	182,210,935 - 182,230,016 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	1	190,571,588 - 190,579,791 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	1	197,757,670 - 197,765,873 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	1	190,428,176 - 190,436,379 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	1	199,052,430 - 199,065,639 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	1	198,894,000 - 199,064,150 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	1	206,075,838 - 206,117,168 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	1	186,894,514 - 186,902,921 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	1	187,046,159 - 187,052,621 (-)	NCBI
Celera	1	179,872,825 - 179,881,028 (-)	NCBI		Celera
Cytogenetic Map	1	q37	NCBI

Znf629
(Chinchilla lanigera - long-tailed chinchilla)

Chinchilla Assembly	Chr	Position (strand)	Source	Genome Browsers
Chinchilla Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChiLan1.0 Ensembl	NW_004955493	7,641,141 - 7,649,927 (-)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955493	7,641,141 - 7,649,927 (-)	NCBI	ChiLan1.0	ChiLan1.0

ZNF629
(Pan paniscus - bonobo/pygmy chimpanzee)

Bonobo Assembly	Chr	Position (strand)	Source	Genome Browsers
Bonobo Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
NHGRI_mPanPan1-v2	18	33,983,862 - 33,996,078 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	16	38,785,321 - 38,797,534 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	16	24,181,152 - 24,191,053 (+)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	16	31,145,520 - 31,154,196 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	16	31,145,520 - 31,154,196 (-)	Ensembl	panpan1.1		panPan2

ZNF629
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	6	17,371,716 - 17,398,895 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	6	17,340,326 - 17,395,541 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	6	18,965,612 - 18,973,899 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	6	17,447,764 - 17,530,691 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	6	17,502,739 - 17,530,683 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	6	17,248,092 - 17,330,971 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	6	17,167,210 - 17,248,671 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	6	17,479,756 - 17,561,472 (+)	NCBI		UU_Cfam_GSD_1.0

Znf629
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)

Squirrel Assembly	Chr	Position (strand)	Source	Genome Browsers
Squirrel Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HiC_Itri_2	NW_024409344	125,072,686 - 125,101,039 (-)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936501	13,170,571 - 13,179,297 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936501	13,170,546 - 13,179,299 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

ZNF629
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	3	17,610,293 - 17,618,999 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	3	17,610,100 - 17,622,577 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	3	18,056,249 - 18,068,098 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

ZNF629
(Chlorocebus sabaeus - green monkey)

Green Monkey Assembly	Chr	Position (strand)	Source	Genome Browsers
Green Monkey Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChlSab1.1	5	27,466,199 - 27,476,063 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	5	27,466,162 - 27,472,607 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666068	2,000,324 - 2,009,155 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Znf629
(Heterocephalus glaber - naked mole-rat)

Naked Mole-Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Naked Mole-Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HetGla_female_1.0 Ensembl	NW_004624782	13,902,342 - 13,905,944 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624782	13,899,232 - 13,906,736 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in ZNF629
39 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 16p11.2-11.1(chr16:30691912-36160463)x3	copy number gain	See cases [RCV000133811]	Chr16:30691912..36160463 [GRCh38] Chr16:30703233..35147508 [GRCh37] Chr16:30610734..35005009 [NCBI36] Chr16:16p11.2-11.1	pathogenic
GRCh38/hg38 16p11.2(chr16:29909613-31438697)x3	copy number gain	See cases [RCV000135339]	Chr16:29909613..31438697 [GRCh38] Chr16:29920934..31450018 [GRCh37] Chr16:29828435..31357519 [NCBI36] Chr16:16p11.2	pathogenic
GRCh38/hg38 16p12.1-11.2(chr16:27311746-31193406)x3	copy number gain	See cases [RCV000140341]	Chr16:27311746..31193406 [GRCh38] Chr16:27323067..31204727 [GRCh37] Chr16:27230568..31112228 [NCBI36] Chr16:16p12.1-11.2	pathogenic
GRCh38/hg38 16p12.2-11.2(chr16:23752047-31943755)x3	copy number gain	See cases [RCV000141141]	Chr16:23752047..31943755 [GRCh38] Chr16:23763368..31955076 [GRCh37] Chr16:23670869..31862577 [NCBI36] Chr16:16p12.2-11.2	pathogenic
GRCh37/hg19 16p11.2(chr16:30391304-31122666)x3	copy number gain	Breast ductal adenocarcinoma [RCV000207028]	Chr16:30391304..31122666 [GRCh37] Chr16:16p11.2	uncertain significance
GRCh37/hg19 16p13.3-11.2(chr16:1279324-31926800)x3	copy number gain	Breast ductal adenocarcinoma [RCV000207053]	Chr16:1279324..31926800 [GRCh37] Chr16:16p13.3-11.2	uncertain significance
NM_001080417.3(ZNF629):c.2596G>C (p.Gly866Arg)	single nucleotide variant	not specified [RCV004319800]	Chr16:30781732 [GRCh38] Chr16:30793053 [GRCh37] Chr16:16p11.2	uncertain significance
Single allele	deletion	Branched-chain keto acid dehydrogenase kinase deficiency [RCV000735205]	Chr16:30554158..31536880 [GRCh37] Chr16:16p11.2	uncertain significance
GRCh37/hg19 16p13.3-q24.3(chr16:69193-90274381)x3	copy number gain	See cases [RCV000446684]	Chr16:69193..90274381 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16p11.2(chr16:30515442-30792856)x1	copy number loss	See cases [RCV000445894]	Chr16:30515442..30792856 [GRCh37] Chr16:16p11.2	uncertain significance
GRCh37/hg19 16p11.2(chr16:28826162-29043901)x1	copy number loss	See cases [RCV000448084]	Chr16:28826162..29043901 [GRCh37] Chr16:16p11.2	likely pathogenic
GRCh37/hg19 16p11.2(chr16:30607048-31117069)x1	copy number loss	See cases [RCV000511454]	Chr16:30607048..31117069 [GRCh37] Chr16:16p11.2	uncertain significance
GRCh37/hg19 16p13.2-q24.3(chr16:9273328-89548493)x3	copy number gain	See cases [RCV000511622]	Chr16:9273328..89548493 [GRCh37] Chr16:16p13.2-q24.3	uncertain significance
maternal UPD(16p)	complex	Hemimegalencephaly [RCV000494707]	Chr16:1280042..33710558 [GRCh37] Chr16:16p13.3-11.2	pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062)	copy number gain	See cases [RCV000511296]	Chr16:85881..90155062 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062)x3	copy number gain	See cases [RCV000512138]	Chr16:85881..90155062 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:88165-90163275)x3	copy number gain	not provided [RCV000738917]	Chr16:88165..90163275 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:88165-90274695)x3	copy number gain	not provided [RCV000738918]	Chr16:88165..90274695 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:61451-90294632)x3	copy number gain	not provided [RCV000738915]	Chr16:61451..90294632 [GRCh37] Chr16:16p13.3-q24.3	pathogenic
GRCh37/hg19 16p11.2(chr16:30738551-34194635)x3	copy number gain	not provided [RCV000739123]	Chr16:30738551..34194635 [GRCh37] Chr16:16p11.2	benign
NM_001080417.3(ZNF629):c.175A>T (p.Thr59Ser)	single nucleotide variant	not provided [RCV000898594]	Chr16:30784153 [GRCh38] Chr16:30795474 [GRCh37] Chr16:16p11.2	benign
NM_001080417.3(ZNF629):c.2480A>T (p.His827Leu)	single nucleotide variant	not provided [RCV000957403]	Chr16:30781848 [GRCh38] Chr16:30793169 [GRCh37] Chr16:16p11.2	benign
NM_001080417.3(ZNF629):c.2306G>C (p.Arg769Pro)	single nucleotide variant	not specified [RCV004313838]	Chr16:30782022 [GRCh38] Chr16:30793343 [GRCh37] Chr16:16p11.2	uncertain significance
GRCh37/hg19 16p13.3-11.2(chr16:5805001-34230001)	copy number gain	Microcephaly [RCV001252948]	Chr16:5805001..34230001 [GRCh37] Chr16:16p13.3-11.2	pathogenic
GRCh37/hg19 16p11.2(chr16:30350747-31905898)x3	copy number gain	not provided [RCV001258619]	Chr16:30350747..31905898 [GRCh37] Chr16:16p11.2	uncertain significance
NC_000016.9:g.(?_30712146)_(31021717_?)dup	duplication	Generalized epilepsy with febrile seizures plus, type 9 [RCV003122990]	Chr16:30712146..31021717 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.1321A>G (p.Met441Val)	single nucleotide variant	not specified [RCV004111639]	Chr16:30783007 [GRCh38] Chr16:30794328 [GRCh37] Chr16:16p11.2	uncertain significance
GRCh37/hg19 16p11.2(chr16:30460206-30906733)x3	copy number gain	not provided [RCV002475788]	Chr16:30460206..30906733 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.1804G>A (p.Gly602Ser)	single nucleotide variant	not specified [RCV004143336]	Chr16:30782524 [GRCh38] Chr16:30793845 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.1668C>A (p.Asp556Glu)	single nucleotide variant	not specified [RCV004205187]	Chr16:30782660 [GRCh38] Chr16:30793981 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.2223C>G (p.Ser741Arg)	single nucleotide variant	not specified [RCV004193085]	Chr16:30782105 [GRCh38] Chr16:30793426 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.338G>C (p.Ser113Thr)	single nucleotide variant	not specified [RCV004083907]	Chr16:30783990 [GRCh38] Chr16:30795311 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.1805G>A (p.Gly602Asp)	single nucleotide variant	not specified [RCV004184329]	Chr16:30782523 [GRCh38] Chr16:30793844 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.2393C>T (p.Pro798Leu)	single nucleotide variant	not specified [RCV004211584]	Chr16:30781935 [GRCh38] Chr16:30793256 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.2455C>G (p.Pro819Ala)	single nucleotide variant	not specified [RCV004115819]	Chr16:30781873 [GRCh38] Chr16:30793194 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.2260G>T (p.Val754Phe)	single nucleotide variant	not specified [RCV004164104]	Chr16:30782068 [GRCh38] Chr16:30793389 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.2449G>A (p.Glu817Lys)	single nucleotide variant	not specified [RCV004190270]	Chr16:30781879 [GRCh38] Chr16:30793200 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.2548G>A (p.Gly850Ser)	single nucleotide variant	not specified [RCV004099594]	Chr16:30781780 [GRCh38] Chr16:30793101 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.113A>G (p.Glu38Gly)	single nucleotide variant	not specified [RCV004194288]	Chr16:30784215 [GRCh38] Chr16:30795536 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.292G>A (p.Glu98Lys)	single nucleotide variant	not specified [RCV004086564]	Chr16:30784036 [GRCh38] Chr16:30795357 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.1664G>C (p.Gly555Ala)	single nucleotide variant	not specified [RCV004267637]	Chr16:30782664 [GRCh38] Chr16:30793985 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.259G>C (p.Asp87His)	single nucleotide variant	not specified [RCV004253814]	Chr16:30784069 [GRCh38] Chr16:30795390 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.2338C>T (p.Arg780Cys)	single nucleotide variant	not specified [RCV004321539]	Chr16:30781990 [GRCh38] Chr16:30793311 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.1928C>T (p.Pro643Leu)	single nucleotide variant	not specified [RCV004365151]	Chr16:30782400 [GRCh38] Chr16:30793721 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.2131G>A (p.Gly711Arg)	single nucleotide variant	not specified [RCV004353026]	Chr16:30782197 [GRCh38] Chr16:30793518 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.1858C>G (p.Pro620Ala)	single nucleotide variant	not specified [RCV004361052]	Chr16:30782470 [GRCh38] Chr16:30793791 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.772G>A (p.Gly258Ser)	single nucleotide variant	not specified [RCV004359699]	Chr16:30783556 [GRCh38] Chr16:30794877 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.1924A>C (p.Lys642Gln)	single nucleotide variant	not specified [RCV004487184]	Chr16:30782404 [GRCh38] Chr16:30793725 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.2437G>A (p.Glu813Lys)	single nucleotide variant	not specified [RCV004487186]	Chr16:30781891 [GRCh38] Chr16:30793212 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.826G>A (p.Asp276Asn)	single nucleotide variant	not specified [RCV004487190]	Chr16:30783502 [GRCh38] Chr16:30794823 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.104C>A (p.Pro35His)	single nucleotide variant	not specified [RCV004487180]	Chr16:30784224 [GRCh38] Chr16:30795545 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.1229G>C (p.Ser410Thr)	single nucleotide variant	not specified [RCV004487181]	Chr16:30783099 [GRCh38] Chr16:30794420 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.2398G>T (p.Asp800Tyr)	single nucleotide variant	not specified [RCV004487185]	Chr16:30781930 [GRCh38] Chr16:30793251 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.326C>T (p.Ala109Val)	single nucleotide variant	not specified [RCV004487188]	Chr16:30784002 [GRCh38] Chr16:30795323 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.385C>T (p.Pro129Ser)	single nucleotide variant	not specified [RCV004487189]	Chr16:30783943 [GRCh38] Chr16:30795264 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.94G>A (p.Glu32Lys)	single nucleotide variant	not specified [RCV004487192]	Chr16:30784234 [GRCh38] Chr16:30795555 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.1634G>A (p.Arg545Lys)	single nucleotide variant	not specified [RCV004487182]	Chr16:30782694 [GRCh38] Chr16:30794015 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.1658G>T (p.Gly553Val)	single nucleotide variant	not specified [RCV004487183]	Chr16:30782670 [GRCh38] Chr16:30793991 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.877C>T (p.Pro293Ser)	single nucleotide variant	not specified [RCV004487191]	Chr16:30783451 [GRCh38] Chr16:30794772 [GRCh37] Chr16:16p11.2	uncertain significance
NC_000016.9:g.(?_28889993)_(31202759_?)del	deletion	Dilated Cardiomyopathy, Dominant [RCV004582801]	Chr16:28889993..31202759 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.2465C>A (p.Thr822Lys)	single nucleotide variant	not specified [RCV004600052]	Chr16:30781863 [GRCh38] Chr16:30793184 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.61G>T (p.Asp21Tyr)	single nucleotide variant	not specified [RCV004600054]	Chr16:30784422 [GRCh38] Chr16:30795743 [GRCh37] Chr16:16p11.2	uncertain significance
NM_001080417.3(ZNF629):c.2284C>A (p.Pro762Thr)	single nucleotide variant	not specified [RCV004600051]	Chr16:30782044 [GRCh38] Chr16:30793365 [GRCh37] Chr16:16p11.2	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	1574
Count of miRNA genes:	834
Interacting mature miRNAs:	989
Transcripts:	ENST00000262525
Prediction methods:	Miranda, Rnahybrid
Result types:	miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Markers in Region

RH65007

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	16	30,791,273 - 30,791,393	UniSTS	GRCh37
Build 36	16	30,698,774 - 30,698,894	RGD	NCBI36
Celera	16	29,506,028 - 29,506,148	RGD
Cytogenetic Map	16	p11.2	UniSTS
HuRef	16	28,354,104 - 28,354,224	UniSTS

Cda1jd07

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	16	30,789,917 - 30,790,036	UniSTS	GRCh37
Build 36	16	30,697,418 - 30,697,537	RGD	NCBI36
Celera	16	29,507,385 - 29,507,504	RGD
Cytogenetic Map	16	p11.2	UniSTS
HuRef	16	28,352,748 - 28,352,867	UniSTS

SHGC-61072

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	16	30,789,793 - 30,790,071	UniSTS	GRCh37
Build 36	16	30,697,294 - 30,697,572	RGD	NCBI36
Celera	16	29,507,350 - 29,507,628	RGD
Cytogenetic Map	16	p11.2	UniSTS
HuRef	16	28,352,624 - 28,352,902	UniSTS

D16S3188

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	16	30,789,804 - 30,789,996	UniSTS	GRCh37
Build 36	16	30,697,305 - 30,697,497	RGD	NCBI36
Celera	16	29,507,425 - 29,507,617	RGD
Cytogenetic Map	16	p11.2	UniSTS
HuRef	16	28,352,635 - 28,352,827	UniSTS

Expression

RNA-SEQ Expression

Click on a value in the shaded box below the category label to view a detailed expression data table for that system.

Download All Expressed Objects for this Gene

adipose tissue	alimentary part of gastrointestinal system	appendage	circulatory system	ectoderm	endocrine system	endoderm	entire extraembryonic component	exocrine system	hemolymphoid system	hepatobiliary system	integumental system	mesenchyme	mesoderm	musculoskeletal system	nervous system	pharyngeal arch	renal system	reproductive system	respiratory system	sensory system	visual system
1204	2439	2788	2250	4973	1725	2350	6	623	1936	464	2269	7293	6460	53	3734	1	852	1744	1617	175	1

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001080417	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001345970	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AA530984	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AB002324	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC106886	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK026115	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC015676	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC047041	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC063520	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC080594	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471192	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068262	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HY083602	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	HY169754	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	M88374	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000262525 ⟹ ENSP00000262525

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	16	30,778,456 - 30,787,205 (-)	Ensembl

RefSeq Acc Id:

NM_001080417 ⟹ NP_001073886

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	30,778,456 - 30,787,205 (-)	NCBI
GRCh37	16	30,789,770 - 30,798,564 (-)	NCBI
Build 36	16	30,697,271 - 30,706,024 (-)	NCBI Archive
Celera	16	29,498,892 - 29,507,651 (+)	RGD
HuRef	16	28,352,601 - 28,361,366 (-)	RGD
CHM1_1	16	32,106,931 - 32,115,684 (-)	NCBI
T2T-CHM13v2.0	16	31,165,899 - 31,174,664 (-)	NCBI

Sequence:

show sequence

ACTTCCTGCTCCGTCCCAGTCACCCTGAACTGGTCCCCGGGTCCTCAGCCTGGAATCACCCCTT
GAGAAGGACCCCAGAGTCCTCGGCGCCCAGTCCGTCCCCCGAGGCAGGGCACTGAAGGGGTTAA
GTCCCCTGGGGCTGGATTCCGCCTTCCGGCTTTTCCCAGACCCCAGAGCCGGTCCCTGGAACAC
TGCAGTCCTGAGCTCTGGGATGGAGCCCGAGACTGCGCTGTGGGGCCCGGATCTGCAGGGTCCG
GAACAGAGCCCCAACGATGCTCACAGAGGTGCCGAGAGTGAAAACGAAGAGGAGAGCCCTCGGC
AGGAAAGTTCTGGGGAGGAGATCATCATGGGAGACCCGGCTCAGAGTCCAGAATCCAAGGACTC
AACAGAGATGTCCCTGGAGAGATCCTCCCAGGACCCCTCTGTCCCCCAGAACCCCCCAACCCCA
CTGGGTCACTCCAATCCCTTGGACCACCAGATCCCCCTGGACCCCCCAGCCCCGGAGGTAGTCC
CTACCCCATCTGACTGGACCAAGGCCTGCGAGGCCAGCTGGCAGTGGGGCGCTCTCACCACATG
GAACAGCCCCCCAGTCGTCCCCGCCAACGAGCCCAGCCTGCGGGAGCTGGTGCAGGGCCGCCCG
GCGGGGGCGGAGAAGCCCTACATCTGCAACGAGTGCGGCAAGAGCTTCAGCCAGTGGTCCAAGC
TGCTGCGGCACCAGCGCATCCACACGGGAGAGCGGCCCAACACCTGCTCCGAGTGCGGCAAGAG
CTTCACGCAGAGCTCGCACCTGGTGCAGCACCAGCGCACGCACACCGGCGAGAAGCCCTACAAG
TGCCCCGACTGCGGCAAGTGCTTCAGCTGGAGCTCCAACCTGGTGCAGCACCAGCGCACGCACA
CGGGAGAGAAGCCCTACAAGTGCACGGAGTGCGAGAAAGCCTTCACCCAGAGCACCAACCTCAT
CAAGCACCAGCGATCCCACACCGGCGAGAAGCCCTACAAGTGCGGCGAGTGCCGCCGGGCTTTC
TACCGCAGCTCGGACCTCATCCAGCACCAGGCCACCCACACAGGCGAGAAACCCTACAAGTGCC
CCGAGTGCGGGAAGCGCTTCGGCCAGAACCACAACCTCCTCAAGCACCAGAAGATCCACGCGGG
CGAGAAGCCATACCGCTGCACCGAGTGCGGGAAGAGCTTCATCCAGAGCTCGGAGCTGACCCAG
CACCAGCGCACGCACACAGGCGAGAAGCCCTACGAGTGCCTAGAGTGCGGCAAGAGCTTCGGCC
ACAGCTCCACCCTCATCAAGCACCAGCGGACTCACCTGCGCGAGGACCCGTTCAAGTGCCCAGT
GTGCGGCAAGACCTTCACCCTGAGCGCCACGTTGCTGCGGCACCAGCGCACGCACACGGGCGAG
CGGCCCTACAAGTGCCCAGAGTGCGGCAAGAGCTTCAGCGTCAGCTCCAACCTCATCAACCACC
AGCGCATCCACCGCGGCGAGCGGCCCTACATCTGCGCCGACTGCGGCAAGAGCTTCATCATGAG
CTCCACCCTTATCCGCCACCAGCGCATCCACACCGGTGAGAAGCCCTACAAGTGTTCCGACTGC
GGCAAGAGCTTCATCCGCAGCTCCCACCTTATCCAGCACCGCCGCACGCACACCGGCGAGAAGC
CCTACAAGTGCCCCGAGTGCGGCAAGAGCTTCAGCCAGAGCTCCAACCTTATTACCCACGTCCG
CACGCACATGGACGAGAACCTGTTCGTGTGCTCCGACTGCGGGAAGGCCTTCCTGGAAGCCCAC
GAGCTGGAGCAGCACCGGGTGATCCATGAGAGGGGGAAGACCCCAGCGCGTAGGGCCCAGGGCG
ACAGCCTGCTGGGGCTCGGGGACCCCTCCCTGCTGACCCCGCCGCCGGGAGCCAAGCCGCACAA
GTGTCTCGTGTGCGGAAAGGGCTTCAACGACGAGGGCATCTTCATGCAACATCAGAGGATCCAC
ATCGGAGAAAACCCCTACAAAAATGCAGACGGCCTCATCGCACACGCAGCCCCCAAACCTCCTC
AGTTACGATCCCCAAGGCTCCCTTTCAGAGGGAATTCCTACCCCGGGGCTGCGGAGGGCAGAGC
GGAGGCCCCCGGACAGCCCCTTAAGCCGCCGGAGGGTCAGGAGGGCTTCAGCCAGAGGCGGGGG
CTGCTGTCCTCCAAGACCTACATCTGCTCCCACTGCGGAGAGAGCTTCCTGGATCGCTCTGTGC
TCCTCCAGCATCAGCTCACCCACGGCAACGAAAAGCCCTTTCTCTTTCCTGATTATAGAATTGG
CCTAGGGGAAGGCGCAGGGCCCAGCCCCTTCTTAAGTGGGAAGCCCTTTAAATGCCCTGAATGC
AAACAAAGCTTTGGCCTCAGCTCTGAGCTGCTGCTGCACCAGAAAGTCCATGCAGGCGGGAAGA
GCTCCCAGAAGAGTCCAGAGCTGGGGAAGAGCTCTTCCGTCCTCCTGGAGCATCTCAGGAGCCC
CCTGGGGGCCAGACCCTACCGCTGCTCAGATTGCAGGGCCTCCTTCCTCGACCGCGTGGCCCTC
ACCCGGCACCAAGAAACCCACACCCAGGAAAAACCCCCCAATCCCGAGGACCCCCCTCCAGAGG
CAGTCACCCTGTCCACAGATCAGGAAGGTGAGGGCGAGACCCCTACCCCCACAGAGAGCAGCAG
CCATGGGGAAGGGCAAAACCCCAAAACCCTAGTGGAAGAAAAGCCCTATCTGTGCCCCGAGTGT
GGAGCCGGCTTCACAGAAGTCGCAGCCCTCCTGCTCCATAGGAGCTGCCACCCAGGTGTCTCCC
TGTGAAATGGGTCTGGAGACCAGGGGCCTCGCTCTCTCCAGAGAGGAACACTGGATTTTTTCCC
CCAAAAAAATTACATGGGGAAGGGAGGATAACCCTATCAGATGGTAGTGGAGTGGAGGAGAAAG
AACCCTGGGAAAAAATAGTGCTTTTACATCAGTGATGAGAAACCCTATAAAATTGTTGGTGGGA
AGCACTTATAAGGCAGTAGAGAAAAACTGTTGGGTTAGAAACCCTATAAATATGTAGGAAAAAA
AAAAGCCCTTTAAGTCTGTAGCAGAAAAACCCTATAAACCATAGTGGATAAAAGCCCTATTAAT
TGTAGGAAGAGGTCCCAATATGTCTCTGAACAACCCTATAAAATTGTATCAAAATCCTTAGGAA
AATCCTATAGGGTCGGGGAAGTACCGCAATGGCACTGACCCGGGAGTAACGACCCTCAGATGAT
GCAGAAAACACCTCTCCCTCACTGTTCCACAATGTTCTCTCCCAGCAGCCCTGGACAGTTCTCA
TGGAGGAAGATGCTCAGCTGGGGGAGTGGTGTGGGAACTGGGTGGAACTGAAAAGGAAGAAAAT
AGGAGAAAAATAAGTGACCAGGAGCTCTGGAGCCCCCAGAGGAGATAAGACAGAGACTAGGAAG
AAAAGGTCCCACTCACTGCACTGGGGTCCTTGGGGTTTGAGGACAATGTTAGATGCATTGTGTG
TTTTAGGGAAAGAGGCCTATGGAATCCCTTATCAAAACCCCAAAATGGGGAAGAAAAAACAAAT
TGGCAAGCCTTTTTAAAGGCTGAAGTTTGGGGTGCAGAAACATGGTCAGTATAAGAATACTGAG
AAACCACCACAAAAATTAGGGGGAAGCAGGGGGCAGTTTCTGTTAGATTGCTTTGAGGGGAGCA
AACCAAGGTGGGGAAACTGCTCACATGGAACCCAGCTAACTCCAGGCCCCTTCTTGCTTCCGGA
AGCTTGCGAAACTGCAAGTAGCAGGCAGGTCCCAGCTCTCAGAGTGCAAGGGTTCTCCCCACAC
CAGGCAGGACCACCCTTTCTCCCTGCCCAGCCAGGGACTTCTACTCTGCAAGGCCTCCAGGGAT
GGCGGTTGCCTCCCACCACATTCTCAGGTCTCACCTTCAGGAGGTTTTTCCTGAAATCTAACTG
CCGCCAGTGGCAGCTCATTTCCTCAAATTCTGTCCTCAGTGGAGAGGGAGAACCGCTGCTAGTC
GACCTCCAAAGAATAAAGCCCTTCAGAGACTTAGGGCCTGCGTGTGGGCCTCCCCAGCCTTCTC
CAAGTCATCAGGGCCACAGAATTTCTTAGAAAGCTTTGATTAGCCAGCAACTTGATTTTAAACT
TCAGCTATTCATCTTTGTTGGTAGCAAGGCTGCCCCGCAGGATAAGGCAGCCCTCCTCCCTGGT
GGGGATCCAGACACCCCACAGACTGAGCCACAGGTCCCTGAAGAGTCCGCAGAGGCCGTATCAC
CCTCTTCACCCTGGTACCTGGAGCCCTCCAGGGTTGTGAGATCCAGCCCAATCTCAGCCTTGAG
ATGGATGGGATGGATTCCACTCACTTGGCTCCCCTCTCCTCCTTAGCCAGAAACCTTCAGAAGG
AAACAGAAGGATGAGAAAGCCTCCCTTGCCAGGCCCATCTCACCTCCCACACCACACAGTTACA
CATTCATAAACAGCCAAGCCTGCTCACAGGCCTGGGCATATGTGGCTGGGGAGAGACTGTTGCC
CTATGAGATGGTGGAAGACAGAAAACTCTTGAATGAAACATCTGTAACAAGACTCCCACTCCCT
AATCCTGGAGACCCCTTCAAAAGGAGAGGACTCTGCTCAGCGCTGGGTCAGAAAGGAAGTGCTT
GCCAACCCCAGTAATGCGCTGTCCTGGAGTAAGAGGACTGAGATGCCAGCTGTGGGGCCCGTCA
GGAGTCACGTCTCAAGAGAGGGGTGACCCAGATTTTTGCAAAGCTGTGGAAGAGACCTCTAATT
CCATGACCTAAAGTTTCACACAACCTTTATGCAAATCCTTCGCCATTTGTCTATCCTGGCCCCA
GCAGGATGACCCTCACATTTAAAAGGATCAAAATCTCAAACATTGTGGGAGGAAAACGCCAGGC
CTGCTGGGGAGAGGGAGAAGGCAGGCCTCAGGATTGTGCGGAGAACCATGTTGCCATCTGCATA
ACGCCCCAGCCTATCCAAGTGCCAGGAAGGGAAGCACTACTGAGGGGGGTGCTGCCTGTGGGTC
TCTTCCTAACAGAACGCCAACGAAGGGGGTGCCCTGTAAGAATGAGAAGTCTGCCAAGTCTAAG
GAGATGTCCCCCTCCCCAAGATGGTAGCAGAAACTGAAGTTGTAAAGACAAACCTCTCGCAAAG
CCAGAAGCAGATGCTCTCAAAAACAGGCCTAAGGAATCTGTTCCCAGAAGAGGCCTGGGGAGCA
GCTTTTGGGGCTCAGAGGCCAGTCTGGGGGGAGGCAGGCAGTGTGACTGAAGGCCGGCGCAGGC
CTGTTTCGGACTAGGGTGTAGCATATTTAGTAGGATGCTCACATGTTGTAGGGATGGGTGAGGG
CTAAGGGGCTTGGCTCTTGTACGGGATGGATGATGTGAGCGCACAGTTCGTAGGGTCAGGCGTC
TTGCGGTAGGAAAGGGGCAGGGTTCGATACCTCTGGGGTGTGGCGTGTTCTCTCTTGCCCACCT
CCCCAAGCTCCTTTAACCAGGAGCTTCCCTCCCAGAGTGAGCTACGTCTTGGGAGGATTGAAGC
AGGGAGGTGGCAGTGGCTAGAGTTGCTCAGATCGGCTCAGATGAAGGCCCAGGGGTCAAAGCAT
TTGCTCACCACAACTGAGTCTGGAAGGCACTGTGCAGCCAAACCCTCTTGTCCAATCACATGCA
GGCCCCAGGCCCCTCAGAAACGCCCTGGTGGAGGGAGGAGCCCAACAGATAGGGTCAGGGAGTC
AGTGGGGAAAGCAGAGGGGAGAGCTTAGAGTGAAACTTGAAACTGCTATGGACATGGAGGTCAG
ATGGGAACTTGGAACTGGGCATGAATCCTGAATGGTGGGGAAACTTGAAGCCATCACAGCCAAG
AGGTGGGGTTCCATGACCTGCCCTGAGGTCAGCAGCTCCCAGACTCCTTTGCCCTCACTAGGGA
AGCCCCAGTCACCGGACTTGTCCCCATGGAGTGAAGAGAGGCCCCATTTTTGAGTGTTGTGTGT
CCAAAACAGTGTTGTGTCACTGGTGGTCATGTTGCTTAGTTGAAGAGAATAAAGGGAATAAGAT
TTC

hide sequence

RefSeq Acc Id:

NM_001345970 ⟹ NP_001332899

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	30,778,456 - 30,787,205 (-)	NCBI
T2T-CHM13v2.0	16	31,165,899 - 31,174,664 (-)	NCBI

Sequence:

show sequence

ACTTCCTGCTCCGTCCCAGTCACCCTGAACTGGTCCCCGGGTCCTCAGCCTGGAATCACCCCTT
GAGAAGGACCCCAGAGTCCTCGGCGCCCAGTCCGTCCCCCGAGGCAGGGCACTGAAGGGGTTAA
GTCCCCTGGGGCTGGATTCCGCCTTCCGGCTTTTCCCAGACCCCAGAGCCGGTCCCTGGAACAC
TGCAGTCCTGAGCTCTGGGATGGAGCCCGAGACTGCGCTGTGGGGCCCGGATCTGCAGGGTCCG
GAACAGAGCCCCAACGATGCTCACAGAGACTCCCTTTCTTTCTGTAGGTGCCGAGAGTGAAAAC
GAAGAGGAGAGCCCTCGGCAGGAAAGTTCTGGGGAGGAGATCATCATGGGAGACCCGGCTCAGA
GTCCAGAATCCAAGGACTCAACAGAGATGTCCCTGGAGAGATCCTCCCAGGACCCCTCTGTCCC
CCAGAACCCCCCAACCCCACTGGGTCACTCCAATCCCTTGGACCACCAGATCCCCCTGGACCCC
CCAGCCCCGGAGGTAGTCCCTACCCCATCTGACTGGACCAAGGCCTGCGAGGCCAGCTGGCAGT
GGGGCGCTCTCACCACATGGAACAGCCCCCCAGTCGTCCCCGCCAACGAGCCCAGCCTGCGGGA
GCTGGTGCAGGGCCGCCCGGCGGGGGCGGAGAAGCCCTACATCTGCAACGAGTGCGGCAAGAGC
TTCAGCCAGTGGTCCAAGCTGCTGCGGCACCAGCGCATCCACACGGGAGAGCGGCCCAACACCT
GCTCCGAGTGCGGCAAGAGCTTCACGCAGAGCTCGCACCTGGTGCAGCACCAGCGCACGCACAC
CGGCGAGAAGCCCTACAAGTGCCCCGACTGCGGCAAGTGCTTCAGCTGGAGCTCCAACCTGGTG
CAGCACCAGCGCACGCACACGGGAGAGAAGCCCTACAAGTGCACGGAGTGCGAGAAAGCCTTCA
CCCAGAGCACCAACCTCATCAAGCACCAGCGATCCCACACCGGCGAGAAGCCCTACAAGTGCGG
CGAGTGCCGCCGGGCTTTCTACCGCAGCTCGGACCTCATCCAGCACCAGGCCACCCACACAGGC
GAGAAACCCTACAAGTGCCCCGAGTGCGGGAAGCGCTTCGGCCAGAACCACAACCTCCTCAAGC
ACCAGAAGATCCACGCGGGCGAGAAGCCATACCGCTGCACCGAGTGCGGGAAGAGCTTCATCCA
GAGCTCGGAGCTGACCCAGCACCAGCGCACGCACACAGGCGAGAAGCCCTACGAGTGCCTAGAG
TGCGGCAAGAGCTTCGGCCACAGCTCCACCCTCATCAAGCACCAGCGGACTCACCTGCGCGAGG
ACCCGTTCAAGTGCCCAGTGTGCGGCAAGACCTTCACCCTGAGCGCCACGTTGCTGCGGCACCA
GCGCACGCACACGGGCGAGCGGCCCTACAAGTGCCCAGAGTGCGGCAAGAGCTTCAGCGTCAGC
TCCAACCTCATCAACCACCAGCGCATCCACCGCGGCGAGCGGCCCTACATCTGCGCCGACTGCG
GCAAGAGCTTCATCATGAGCTCCACCCTTATCCGCCACCAGCGCATCCACACCGGTGAGAAGCC
CTACAAGTGTTCCGACTGCGGCAAGAGCTTCATCCGCAGCTCCCACCTTATCCAGCACCGCCGC
ACGCACACCGGCGAGAAGCCCTACAAGTGCCCCGAGTGCGGCAAGAGCTTCAGCCAGAGCTCCA
ACCTTATTACCCACGTCCGCACGCACATGGACGAGAACCTGTTCGTGTGCTCCGACTGCGGGAA
GGCCTTCCTGGAAGCCCACGAGCTGGAGCAGCACCGGGTGATCCATGAGAGGGGGAAGACCCCA
GCGCGTAGGGCCCAGGGCGACAGCCTGCTGGGGCTCGGGGACCCCTCCCTGCTGACCCCGCCGC
CGGGAGCCAAGCCGCACAAGTGTCTCGTGTGCGGAAAGGGCTTCAACGACGAGGGCATCTTCAT
GCAACATCAGAGGATCCACATCGGAGAAAACCCCTACAAAAATGCAGACGGCCTCATCGCACAC
GCAGCCCCCAAACCTCCTCAGTTACGATCCCCAAGGCTCCCTTTCAGAGGGAATTCCTACCCCG
GGGCTGCGGAGGGCAGAGCGGAGGCCCCCGGACAGCCCCTTAAGCCGCCGGAGGGTCAGGAGGG
CTTCAGCCAGAGGCGGGGGCTGCTGTCCTCCAAGACCTACATCTGCTCCCACTGCGGAGAGAGC
TTCCTGGATCGCTCTGTGCTCCTCCAGCATCAGCTCACCCACGGCAACGAAAAGCCCTTTCTCT
TTCCTGATTATAGAATTGGCCTAGGGGAAGGCGCAGGGCCCAGCCCCTTCTTAAGTGGGAAGCC
CTTTAAATGCCCTGAATGCAAACAAAGCTTTGGCCTCAGCTCTGAGCTGCTGCTGCACCAGAAA
GTCCATGCAGGCGGGAAGAGCTCCCAGAAGAGTCCAGAGCTGGGGAAGAGCTCTTCCGTCCTCC
TGGAGCATCTCAGGAGCCCCCTGGGGGCCAGACCCTACCGCTGCTCAGATTGCAGGGCCTCCTT
CCTCGACCGCGTGGCCCTCACCCGGCACCAAGAAACCCACACCCAGGAAAAACCCCCCAATCCC
GAGGACCCCCCTCCAGAGGCAGTCACCCTGTCCACAGATCAGGAAGGTGAGGGCGAGACCCCTA
CCCCCACAGAGAGCAGCAGCCATGGGGAAGGGCAAAACCCCAAAACCCTAGTGGAAGAAAAGCC
CTATCTGTGCCCCGAGTGTGGAGCCGGCTTCACAGAAGTCGCAGCCCTCCTGCTCCATAGGAGC
TGCCACCCAGGTGTCTCCCTGTGAAATGGGTCTGGAGACCAGGGGCCTCGCTCTCTCCAGAGAG
GAACACTGGATTTTTTCCCCCAAAAAAATTACATGGGGAAGGGAGGATAACCCTATCAGATGGT
AGTGGAGTGGAGGAGAAAGAACCCTGGGAAAAAATAGTGCTTTTACATCAGTGATGAGAAACCC
TATAAAATTGTTGGTGGGAAGCACTTATAAGGCAGTAGAGAAAAACTGTTGGGTTAGAAACCCT
ATAAATATGTAGGAAAAAAAAAAGCCCTTTAAGTCTGTAGCAGAAAAACCCTATAAACCATAGT
GGATAAAAGCCCTATTAATTGTAGGAAGAGGTCCCAATATGTCTCTGAACAACCCTATAAAATT
GTATCAAAATCCTTAGGAAAATCCTATAGGGTCGGGGAAGTACCGCAATGGCACTGACCCGGGA
GTAACGACCCTCAGATGATGCAGAAAACACCTCTCCCTCACTGTTCCACAATGTTCTCTCCCAG
CAGCCCTGGACAGTTCTCATGGAGGAAGATGCTCAGCTGGGGGAGTGGTGTGGGAACTGGGTGG
AACTGAAAAGGAAGAAAATAGGAGAAAAATAAGTGACCAGGAGCTCTGGAGCCCCCAGAGGAGA
TAAGACAGAGACTAGGAAGAAAAGGTCCCACTCACTGCACTGGGGTCCTTGGGGTTTGAGGACA
ATGTTAGATGCATTGTGTGTTTTAGGGAAAGAGGCCTATGGAATCCCTTATCAAAACCCCAAAA
TGGGGAAGAAAAAACAAATTGGCAAGCCTTTTTAAAGGCTGAAGTTTGGGGTGCAGAAACATGG
TCAGTATAAGAATACTGAGAAACCACCACAAAAATTAGGGGGAAGCAGGGGGCAGTTTCTGTTA
GATTGCTTTGAGGGGAGCAAACCAAGGTGGGGAAACTGCTCACATGGAACCCAGCTAACTCCAG
GCCCCTTCTTGCTTCCGGAAGCTTGCGAAACTGCAAGTAGCAGGCAGGTCCCAGCTCTCAGAGT
GCAAGGGTTCTCCCCACACCAGGCAGGACCACCCTTTCTCCCTGCCCAGCCAGGGACTTCTACT
CTGCAAGGCCTCCAGGGATGGCGGTTGCCTCCCACCACATTCTCAGGTCTCACCTTCAGGAGGT
TTTTCCTGAAATCTAACTGCCGCCAGTGGCAGCTCATTTCCTCAAATTCTGTCCTCAGTGGAGA
GGGAGAACCGCTGCTAGTCGACCTCCAAAGAATAAAGCCCTTCAGAGACTTAGGGCCTGCGTGT
GGGCCTCCCCAGCCTTCTCCAAGTCATCAGGGCCACAGAATTTCTTAGAAAGCTTTGATTAGCC
AGCAACTTGATTTTAAACTTCAGCTATTCATCTTTGTTGGTAGCAAGGCTGCCCCGCAGGATAA
GGCAGCCCTCCTCCCTGGTGGGGATCCAGACACCCCACAGACTGAGCCACAGGTCCCTGAAGAG
TCCGCAGAGGCCGTATCACCCTCTTCACCCTGGTACCTGGAGCCCTCCAGGGTTGTGAGATCCA
GCCCAATCTCAGCCTTGAGATGGATGGGATGGATTCCACTCACTTGGCTCCCCTCTCCTCCTTA
GCCAGAAACCTTCAGAAGGAAACAGAAGGATGAGAAAGCCTCCCTTGCCAGGCCCATCTCACCT
CCCACACCACACAGTTACACATTCATAAACAGCCAAGCCTGCTCACAGGCCTGGGCATATGTGG
CTGGGGAGAGACTGTTGCCCTATGAGATGGTGGAAGACAGAAAACTCTTGAATGAAACATCTGT
AACAAGACTCCCACTCCCTAATCCTGGAGACCCCTTCAAAAGGAGAGGACTCTGCTCAGCGCTG
GGTCAGAAAGGAAGTGCTTGCCAACCCCAGTAATGCGCTGTCCTGGAGTAAGAGGACTGAGATG
CCAGCTGTGGGGCCCGTCAGGAGTCACGTCTCAAGAGAGGGGTGACCCAGATTTTTGCAAAGCT
GTGGAAGAGACCTCTAATTCCATGACCTAAAGTTTCACACAACCTTTATGCAAATCCTTCGCCA
TTTGTCTATCCTGGCCCCAGCAGGATGACCCTCACATTTAAAAGGATCAAAATCTCAAACATTG
TGGGAGGAAAACGCCAGGCCTGCTGGGGAGAGGGAGAAGGCAGGCCTCAGGATTGTGCGGAGAA
CCATGTTGCCATCTGCATAACGCCCCAGCCTATCCAAGTGCCAGGAAGGGAAGCACTACTGAGG
GGGGTGCTGCCTGTGGGTCTCTTCCTAACAGAACGCCAACGAAGGGGGTGCCCTGTAAGAATGA
GAAGTCTGCCAAGTCTAAGGAGATGTCCCCCTCCCCAAGATGGTAGCAGAAACTGAAGTTGTAA
AGACAAACCTCTCGCAAAGCCAGAAGCAGATGCTCTCAAAAACAGGCCTAAGGAATCTGTTCCC
AGAAGAGGCCTGGGGAGCAGCTTTTGGGGCTCAGAGGCCAGTCTGGGGGGAGGCAGGCAGTGTG
ACTGAAGGCCGGCGCAGGCCTGTTTCGGACTAGGGTGTAGCATATTTAGTAGGATGCTCACATG
TTGTAGGGATGGGTGAGGGCTAAGGGGCTTGGCTCTTGTACGGGATGGATGATGTGAGCGCACA
GTTCGTAGGGTCAGGCGTCTTGCGGTAGGAAAGGGGCAGGGTTCGATACCTCTGGGGTGTGGCG
TGTTCTCTCTTGCCCACCTCCCCAAGCTCCTTTAACCAGGAGCTTCCCTCCCAGAGTGAGCTAC
GTCTTGGGAGGATTGAAGCAGGGAGGTGGCAGTGGCTAGAGTTGCTCAGATCGGCTCAGATGAA
GGCCCAGGGGTCAAAGCATTTGCTCACCACAACTGAGTCTGGAAGGCACTGTGCAGCCAAACCC
TCTTGTCCAATCACATGCAGGCCCCAGGCCCCTCAGAAACGCCCTGGTGGAGGGAGGAGCCCAA
CAGATAGGGTCAGGGAGTCAGTGGGGAAAGCAGAGGGGAGAGCTTAGAGTGAAACTTGAAACTG
CTATGGACATGGAGGTCAGATGGGAACTTGGAACTGGGCATGAATCCTGAATGGTGGGGAAACT
TGAAGCCATCACAGCCAAGAGGTGGGGTTCCATGACCTGCCCTGAGGTCAGCAGCTCCCAGACT
CCTTTGCCCTCACTAGGGAAGCCCCAGTCACCGGACTTGTCCCCATGGAGTGAAGAGAGGCCCC
ATTTTTGAGTGTTGTGTGTCCAAAACAGTGTTGTGTCACTGGTGGTCATGTTGCTTAGTTGAAG
AGAATAAAGGGAATAAGATTTC

hide sequence

Protein Sequences


Protein RefSeqs	NP_001073886	(Get FASTA)	NCBI Sequence Viewer
	NP_001332899	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAA61332	(Get FASTA)	NCBI Sequence Viewer
	BAA20784	(Get FASTA)	NCBI Sequence Viewer
	EAW52195	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000262525
	ENSP00000262525.4
GenBank Protein	Q9UEG4	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_001073886 ⟸ NM_001080417
- Peptide Label:	isoform 1
- UniProtKB:	Q15938 (UniProtKB/Swiss-Prot), Q9UEG4 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MEPETALWGPDLQGPEQSPNDAHRGAESENEEESPRQESSGEEIIMGDPAQSPESKDSTEMSLE RSSQDPSVPQNPPTPLGHSNPLDHQIPLDPPAPEVVPTPSDWTKACEASWQWGALTTWNSPPVV PANEPSLRELVQGRPAGAEKPYICNECGKSFSQWSKLLRHQRIHTGERPNTCSECGKSFTQSSH LVQHQRTHTGEKPYKCPDCGKCFSWSSNLVQHQRTHTGEKPYKCTECEKAFTQSTNLIKHQRSH TGEKPYKCGECRRAFYRSSDLIQHQATHTGEKPYKCPECGKRFGQNHNLLKHQKIHAGEKPYRC TECGKSFIQSSELTQHQRTHTGEKPYECLECGKSFGHSSTLIKHQRTHLREDPFKCPVCGKTFT LSATLLRHQRTHTGERPYKCPECGKSFSVSSNLINHQRIHRGERPYICADCGKSFIMSSTLIRH QRIHTGEKPYKCSDCGKSFIRSSHLIQHRRTHTGEKPYKCPECGKSFSQSSNLITHVRTHMDEN LFVCSDCGKAFLEAHELEQHRVIHERGKTPARRAQGDSLLGLGDPSLLTPPPGAKPHKCLVCGK GFNDEGIFMQHQRIHIGENPYKNADGLIAHAAPKPPQLRSPRLPFRGNSYPGAAEGRAEAPGQP LKPPEGQEGFSQRRGLLSSKTYICSHCGESFLDRSVLLQHQLTHGNEKPFLFPDYRIGLGEGAG PSPFLSGKPFKCPECKQSFGLSSELLLHQKVHAGGKSSQKSPELGKSSSVLLEHLRSPLGARPY RCSDCRASFLDRVALTRHQETHTQEKPPNPEDPPPEAVTLSTDQEGEGETPTPTESSSHGEGQN PKTLVEEKPYLCPECGAGFTEVAALLLHRSCHPGVSL hide sequence

RefSeq Acc Id:	NP_001332899 ⟸ NM_001345970
- Peptide Label:	isoform 2
- UniProtKB:	Q9UEG4 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MLTETPFLSVGAESENEEESPRQESSGEEIIMGDPAQSPESKDSTEMSLERSSQDPSVPQNPPT PLGHSNPLDHQIPLDPPAPEVVPTPSDWTKACEASWQWGALTTWNSPPVVPANEPSLRELVQGR PAGAEKPYICNECGKSFSQWSKLLRHQRIHTGERPNTCSECGKSFTQSSHLVQHQRTHTGEKPY KCPDCGKCFSWSSNLVQHQRTHTGEKPYKCTECEKAFTQSTNLIKHQRSHTGEKPYKCGECRRA FYRSSDLIQHQATHTGEKPYKCPECGKRFGQNHNLLKHQKIHAGEKPYRCTECGKSFIQSSELT QHQRTHTGEKPYECLECGKSFGHSSTLIKHQRTHLREDPFKCPVCGKTFTLSATLLRHQRTHTG ERPYKCPECGKSFSVSSNLINHQRIHRGERPYICADCGKSFIMSSTLIRHQRIHTGEKPYKCSD CGKSFIRSSHLIQHRRTHTGEKPYKCPECGKSFSQSSNLITHVRTHMDENLFVCSDCGKAFLEA HELEQHRVIHERGKTPARRAQGDSLLGLGDPSLLTPPPGAKPHKCLVCGKGFNDEGIFMQHQRI HIGENPYKNADGLIAHAAPKPPQLRSPRLPFRGNSYPGAAEGRAEAPGQPLKPPEGQEGFSQRR GLLSSKTYICSHCGESFLDRSVLLQHQLTHGNEKPFLFPDYRIGLGEGAGPSPFLSGKPFKCPE CKQSFGLSSELLLHQKVHAGGKSSQKSPELGKSSSVLLEHLRSPLGARPYRCSDCRASFLDRVA LTRHQETHTQEKPPNPEDPPPEAVTLSTDQEGEGETPTPTESSSHGEGQNPKTLVEEKPYLCPE CGAGFTEVAALLLHRSCHPGVSL hide sequence

Ensembl Acc Id:

ENSP00000262525 ⟸ ENST00000262525

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q9UEG4-F1-model_v2	AlphaFold	Q9UEG4	1-869	view protein structure

Promoters

RGD ID:

6815125

Promoter ID:

HG_MRA:6002

Type:

Non-CpG

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

K562

Transcripts:

AK026115, BC080594

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	16	30,699,251 - 30,699,751 (-)	MPROMDB

RGD ID:

6793640

Promoter ID:

HG_KWN:23572

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, HeLa_S3, K562, Lymphoblastoid, NB4

Transcripts:

NM_001080417

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	16	30,705,754 - 30,706,254 (-)	MPROMDB

RGD ID:

7232025

Promoter ID:

EPDNEW_H21758

Type:

initiation region

Name:

ZNF629_1

Description:

zinc finger protein 629

SO ACC ID:

SO:0000170

Source:

EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Alternative Promoters:

null; see alsoEPDNEW_H21759

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	30,787,188 - 30,787,248	EPDNEW

RGD ID:

7232027

Promoter ID:

EPDNEW_H21759

Type:

initiation region

Name:

ZNF629_2

Description:

zinc finger protein 629

SO ACC ID:

SO:0000170

Source:

EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Alternative Promoters:

null; see alsoEPDNEW_H21758

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	16	30,787,454 - 30,787,514	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:29008	AgrOrtholog
COSMIC	ZNF629	COSMIC
Ensembl Genes	ENSG00000102870	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript	ENST00000262525	ENTREZGENE
	ENST00000262525.6	UniProtKB/Swiss-Prot
Gene3D-CATH	Classic Zinc Finger	UniProtKB/Swiss-Prot
GTEx	ENSG00000102870	GTEx
HGNC ID	HGNC:29008	ENTREZGENE
Human Proteome Map	ZNF629	Human Proteome Map
InterPro	Znf_C2H2_sf	UniProtKB/Swiss-Prot
	Znf_C2H2_type	UniProtKB/Swiss-Prot
KEGG Report	hsa:23361	UniProtKB/Swiss-Prot
NCBI Gene	23361	ENTREZGENE
OMIM	619587	OMIM
PANTHER	ZINC FINGER AND SCAN DOMAIN-CONTAINING	UniProtKB/Swiss-Prot
	ZINC FINGER PROTEIN 983	UniProtKB/Swiss-Prot
Pfam	zf-C2H2	UniProtKB/Swiss-Prot
PharmGKB	PA134930939	PharmGKB
PROSITE	ZINC_FINGER_C2H2_1	UniProtKB/Swiss-Prot
	ZINC_FINGER_C2H2_2	UniProtKB/Swiss-Prot
SMART	ZnF_C2H2	UniProtKB/Swiss-Prot
Superfamily-SCOP	SSF57667	UniProtKB/Swiss-Prot
UniProt	Q15938	ENTREZGENE
	Q9UEG4	ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary	Q15938	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2016-03-25	ZNF629	zinc finger protein 629	ZNF65	zinc finger protein 65	Data merged from RGD:1350374	737654	PROVISIONAL

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

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